An invariant T cell receptor alpha chain is used by a unique subset of major histocompatibility complex class I-specific CD4+ and CD4-8- T cells in mice and humans.
An invariant T cell receptor alpha chain is used by a unique subset of major histocompatibility complex class I-specific CD4+ and CD4-8- T cells in mice and humans.
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不变的T细胞受体α链由小鼠和人类的主要组织相容性复合物I类CD4+和CD4-8-T细胞的独特子集使用。
DOI:
10.1084/jem.180.3.1097
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发表时间:
1994-09-01
影响因子:
15.3
通讯作者:
Bendelac, Albert
中科院分区:
文献类型:
--
作者:
Lantz, Olivier;Bendelac, Albert
The mouse thymus contains a mature T cell subset that is distinguishable from the mainstream thymocytes by several characteristics. It is restricted in its usage of T cell receptor (TCR) V beta genes to V beta 8, V beta 7, and V beta 2. Its surface phenotype is that of activated/memory cells. It carries the natural killer NK1.1 surface marker. Furthermore, though it consists entirely of CD4+ and CD4-8- cells, its selection in the thymus depends solely upon major histocompatibility complex (MHC) class I expression by cells of hematopoietic origin. Forced persistence of CD8, in fact, imparts negative selection. Here, we have studied the TCR repertoire of this subset and found that, whereas the beta chain V-D-J junctions are quite variable, a single invariant alpha chain V alpha 14-J281 is used by a majority of the TCRs. This surprisingly restricted usage of the V alpha 14-J281 alpha chain is dependent on MHC class I expression, but independent of the MHC haplotype. In humans, a similar unusual population including CD4-8- cells can also be found that uses a strikingly homologous, invariant alpha chain V alpha 24-JQ. Thus, this unique V alpha-J alpha combination has been conserved in both species, conferring specificity to some shared nonpolymorphic MHC class I/peptide self-ligand(s). This implies that the T cell subset that it defines has a specialized and important role, perhaps related to its unique ability to secrete a large set of lymphokines including interleukin 4, upon primary stimulation in vitro and in vivo.
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影响因子:
56.9
作者:
GRUSBY, MJ;JOHNSON, RS;GLIMCHER, LH
通讯作者:
GLIMCHER, LH
影响因子:
15.3
作者:
HAYAKAWA, K;LIN, BT;HARDY, RR
通讯作者:
HARDY, RR
影响因子:
15.3
作者:
BOITEL, B;ERMONVAL, M;ACUTO, O
通讯作者:
ACUTO, O
影响因子:
64.8
作者:
ASARNOW, DM;CADO, D;RAULET, DH
通讯作者:
RAULET, DH
DOI:
10.1073/pnas.87.14.5248
发表时间:
1990-07-01
影响因子:
11.1
作者:
KOSEKI, H;IMAI, K;TANIGUCHI, M
通讯作者:
TANIGUCHI, M